US Drug Recall Register
Class III · Low risk Terminated Initiated Sep 6, 2019 (7 years ago)

Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

GMP Deviation: lot not intended for commercial distribution.

What was recalled

Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets, 240 mg, 30 count bottle, Rx only, Manufactured by: Actabis Laboratories FL, Inc., Fort Lauderdale, FL, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 52544-692-30

Recalling firm
Teva Pharmaceuticals USA
NDC code
52544-692-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0131-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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